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Pharmaceutical Industry Automatic Bottle Syrup Filling Capping Labeling and Packing Production Line
US$20,000.00-150,000.00
1 Piece
Product profile
After-sales Service
Field Installation, Commissioning and TrainingCertification
CE, GMP, ISOCondition
NewModel NO.
customizedCustomized
CustomizedVoltage
380VWarranty
1 YearFinished Dosage Form
LiquidPrecision
High PrecisionComputerized
ComputerizedFilling Volume
30-500mlCapacity
10-60 Bottles/MinFilling Accuracy
≤±1%Pass Rate
≤98%Power Supply
1pH 220V, 50/60HzFilling Head Number
4-8-12Transport Package
Wooden CaseSpecification
9000*2000*2100 mmTrademark
IVENOrigin
ChinaProduction Capacity
CustomizedKey features
Full Customization Options: Offers full customization, minor customization, and flexible customization from samples or designs.
GMP and CE Certified: Manufactured in accordance with GMP, FDA, WHO, CE, and ISO standards.
Advanced Bottle Washing: Features ultrasonic washing, flushing, and optional air charging, drying, and sterilizing.
Flexible Production Capacity: Capacity ranges from 10 to 60 bottles per minute with adjustable filling heads.
Comprehensive After-Sales Support: Includes 24-hour response, on-site installation, training, and engineer dispatch for 6-12 months.
1-Year Warranty Coverage: Provides a 1-year warranty for the machine to ensure long-term operational reliability.
Company profile
CertifiedBusiness Type: Manufacturer/Factory & Trading Company CertifiedCustomization Options: Customization from Samples, Customization from Designs, etc. CertifiedExport Year: 19 Years CertifiedNearest Port: Shanghai PortAverage Response Time: ≤1.49h CertifiedTerms of Payment: LC, T/T, D/P, etc.
AI-Powered supplier vetting
SummaryThe supplier is a combined company offering pharmaceutical and medical production equipment, including vial, ampoule, prefilled syringe, oral liquid, tablet, capsule, visual inspection, packaging, and logistics solutions. It provides extensive customization and integrated services such as process design, equipment selection, installation, commissioning, and validation. Export activity is substantial, with 71%–90% of sales from exports and 19 years of export experience. Quality assurance, ISO9001:2015 certification, CE capability, manufacturing contracts, and finished-product inspection instructions are documented strengths. However, the supplier lacks in-stock, overseas warehouse, overseas showroom, overseas agent or branch capabilities, and has no written procedures for service assessment, corrective actions, or complaint handling. R&D evidence is limited: no SDK, no new products in the past year, and no ODM or major-brand OEM services. No specific customer cases are provided.
CertificationsThe supplier reports an ISO9001:2015 certificate and CE certification capability, providing explicit evidence of quality-management and product-compliance credentials. However, the slices do not specify the scope, validity period, or products covered by these credentials.
After-Sales capabilityThe supplier lists installation, commissioning, validation, maintenance, debugging, repair, training, and integrated consulting services, and provides equipment installation-related offerings. Nevertheless, it has no overseas agents or branches, no overseas warehouse or showroom, and no written procedures or records for complaint handling, service assessment, or corrective and preventive actions, indicating an operational weakness in documented after-sales management.
R&D capabilityThe supplier has customization-oriented R&D services, but reports no available SDK, no new products during the past year, no ODM service, and no OEM service for popular brands. These explicit limitations indicate weak evidence of current product innovation and platform development.
Production capacityThe supplier covers multiple pharmaceutical equipment production lines, including vial and ampoule, prefilled syringe and cartridge, oral liquid, tablet and capsule, inspection, packaging, and logistics systems. It has valid manufacturing contracts with each affiliated subcontractor, follows finished-product inspection instructions uniformly, and reports quality assurance, although no quantitative production-capacity data is provided.
Customization capabilityThe supplier explicitly offers customization from samples, designs, full customization, minor customization, and flexible customization. Its integrated solution includes process design, conceptual and construction design, equipment selection, model customization, installation, commissioning, and validation, demonstrating broad customization coverage.
Product Q&A
Q:Can you customize the machine according to our requirements?
A:
Yes, we offer full customization, minor customization, and flexible customization from samples or designs.
Q:Is your equipment in accordance with GMP, FDA, WHO?
A:
Yes, we design and manufacture equipment according to the GMP, FDA, and WHO requirements of your country.
Q:What are your payment terms?
A:
Generally, we accept TT or irrevocable L/C at sight.
Q:How about your after-sales service?
A:
We reply within 24 hours via email or phone. If a local agent is available, we arrange them to your site within 24 hours. We also provide know-how transfer and dispatch engineers for 6-12 months.
Q:What kind of staff training do you offer?
A:
We train your staff during installation at your site, and you are welcome to send your staff to our factory for training.
Send Inquiry
*To:
Shanghai Iven Pharmatech Engineering Co., Ltd.
Shanghai Iven Pharmatech Engineering Co., Ltd.*Content:
Supplier replies will be sent to your registered email
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